Be aware that beryllium is also quite toxic.

https://en.wikipedia.org/wiki/Acute_beryllium_poisoning

Diana

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Diana R. Tomchick
Professor
Departments of Biophysics and Biochemistry
UT Southwestern Medical Center
5323 Harry Hines Blvd.
Rm. ND10.214A
Dallas, TX 75390-8816
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________________________________
From: CCP4 bulletin board <CCP4BB@JISCMAIL.AC.UK> on behalf of Dr. Kevin M Jude 
<kj...@stanford.edu>
Sent: Friday, January 5, 2024 1:51 PM
To: CCP4BB@JISCMAIL.AC.UK <CCP4BB@JISCMAIL.AC.UK>
Subject: Re: [ccp4bb] How to make GDP.BeF3 solution ?


EXTERNAL MAIL

Nb, dissolution of BeCl2 in water is quite exothermic and releases HCl vapor, 
you will want to prepare that stock in a fume hood.



Best wishes

Kevin



From: CCP4 bulletin board <CCP4BB@JISCMAIL.AC.UK> on behalf of Matthew BOWLER 
<mbow...@embl.fr>
Date: Thursday, January 4, 2024 at 2:19 AM
To: CCP4BB@JISCMAIL.AC.UK <CCP4BB@JISCMAIL.AC.UK>
Subject: Re: [ccp4bb] How to make GDP.BeF3 solution ?

Dear Firdous,

beryllium fluoride is actually a ground state analogue of GTP as 
trifluoroberyllate is tetrahedral. To get a transition sate analogue you need 
either AlF4- or MgF3-. Preparation of these complexes is very easy. The great 
advantage of metal fluoride transition state analogue and ground state analogue 
complexes is the fact that all components are present in solution and readily 
self-assemble in the active site forming stable enzyme complexes that are 
relevant to the catalytic cycle. The inorganic metal fluoride salts (AlF3, and 
MgF2) are too insoluble to use; therefore, the fluoride anion and metal cation 
components must be added from separate stock solutions. Both ammonium fluoride 
and sodium fluoride are suitable as the source of fluoride and are readily 
soluble in water. Metal chlorides can be easily dissolved in water at high 
concentration (0.5 M) and the solutions conserved at -20°C. One of the critical 
aspects in preparing metal fluoride enzyme complexes is the pH of the resulting 
solution. In particular, solutions of AlCl3 and BeCl2 are highly acidic (pH 2) 
samples should be prepared in 100 mM unbuffered Tris base. The optimized 
sequence of component addition is to add fluoride to the prepared buffer first, 
then the metal chloride stock.

Hope this helps, Matt











On 02/01/2024 18:53, Firdous Tarique wrote:

Hi



I would appreciate it if someone could share with me a step by step protocol 
for making a stable GDP.BeF3 solution which is often used as a transition state 
analogue for structural studies of a protein complex ?



Or a vendor from where it can be purchased directly.



Regards



Firdous



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